UA119780C2 - Спосіб одержання диметилдисульфіду - Google Patents
Спосіб одержання диметилдисульфіду Download PDFInfo
- Publication number
- UA119780C2 UA119780C2 UAA201700970A UAA201700970A UA119780C2 UA 119780 C2 UA119780 C2 UA 119780C2 UA A201700970 A UAA201700970 A UA A201700970A UA A201700970 A UAA201700970 A UA A201700970A UA 119780 C2 UA119780 C2 UA 119780C2
- Authority
- UA
- Ukraine
- Prior art keywords
- stage
- hydrogen
- hydrogen sulfide
- reaction
- sulfur
- Prior art date
Links
- 238000000034 method Methods 0.000 title claims abstract description 89
- WQOXQRCZOLPYPM-UHFFFAOYSA-N dimethyl disulfide Chemical compound CSSC WQOXQRCZOLPYPM-UHFFFAOYSA-N 0.000 title claims abstract description 31
- LSDPWZHWYPCBBB-UHFFFAOYSA-N Methanethiol Chemical compound SC LSDPWZHWYPCBBB-UHFFFAOYSA-N 0.000 claims abstract description 89
- RWSOTUBLDIXVET-UHFFFAOYSA-N Dihydrogen sulfide Chemical compound S RWSOTUBLDIXVET-UHFFFAOYSA-N 0.000 claims abstract description 78
- QGJOPFRUJISHPQ-UHFFFAOYSA-N Carbon disulfide Chemical compound S=C=S QGJOPFRUJISHPQ-UHFFFAOYSA-N 0.000 claims abstract description 53
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 claims abstract description 41
- 239000001257 hydrogen Substances 0.000 claims abstract description 37
- 229910052739 hydrogen Inorganic materials 0.000 claims abstract description 37
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims abstract description 27
- 150000002431 hydrogen Chemical class 0.000 claims abstract description 13
- 238000005984 hydrogenation reaction Methods 0.000 claims abstract description 9
- 238000006243 chemical reaction Methods 0.000 claims description 77
- 229910000037 hydrogen sulfide Inorganic materials 0.000 claims description 63
- VNWKTOKETHGBQD-UHFFFAOYSA-N methane Chemical compound C VNWKTOKETHGBQD-UHFFFAOYSA-N 0.000 claims description 58
- 239000011593 sulfur Substances 0.000 claims description 39
- 229910052717 sulfur Inorganic materials 0.000 claims description 39
- 230000015572 biosynthetic process Effects 0.000 claims description 25
- 238000004064 recycling Methods 0.000 claims description 6
- 230000000737 periodic effect Effects 0.000 claims description 3
- 238000010438 heat treatment Methods 0.000 claims description 2
- 238000011437 continuous method Methods 0.000 claims 1
- 150000002430 hydrocarbons Chemical class 0.000 abstract description 43
- 229930195733 hydrocarbon Natural products 0.000 abstract description 42
- 239000004215 Carbon black (E152) Substances 0.000 abstract description 41
- 239000005864 Sulphur Substances 0.000 abstract 2
- 230000003134 recirculating effect Effects 0.000 abstract 2
- 239000003054 catalyst Substances 0.000 description 46
- 230000008569 process Effects 0.000 description 20
- 238000003786 synthesis reaction Methods 0.000 description 18
- 239000007789 gas Substances 0.000 description 17
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 15
- QMMFVYPAHWMCMS-UHFFFAOYSA-N Dimethyl sulfide Chemical compound CSC QMMFVYPAHWMCMS-UHFFFAOYSA-N 0.000 description 13
- 239000000203 mixture Substances 0.000 description 13
- BASFCYQUMIYNBI-UHFFFAOYSA-N platinum Chemical compound [Pt] BASFCYQUMIYNBI-UHFFFAOYSA-N 0.000 description 13
- UGFAIRIUMAVXCW-UHFFFAOYSA-N Carbon monoxide Chemical compound [O+]#[C-] UGFAIRIUMAVXCW-UHFFFAOYSA-N 0.000 description 12
- 229910002091 carbon monoxide Inorganic materials 0.000 description 12
- 229910052751 metal Inorganic materials 0.000 description 11
- 239000002184 metal Substances 0.000 description 11
- 239000000047 product Substances 0.000 description 11
- 238000004519 manufacturing process Methods 0.000 description 10
- 239000007788 liquid Substances 0.000 description 9
- KDLHZDBZIXYQEI-UHFFFAOYSA-N Palladium Chemical compound [Pd] KDLHZDBZIXYQEI-UHFFFAOYSA-N 0.000 description 8
- 230000008901 benefit Effects 0.000 description 8
- 239000011541 reaction mixture Substances 0.000 description 8
- CURLTUGMZLYLDI-UHFFFAOYSA-N Carbon dioxide Chemical compound O=C=O CURLTUGMZLYLDI-UHFFFAOYSA-N 0.000 description 6
- ATUOYWHBWRKTHZ-UHFFFAOYSA-N Propane Chemical compound CCC ATUOYWHBWRKTHZ-UHFFFAOYSA-N 0.000 description 6
- 150000001875 compounds Chemical class 0.000 description 6
- 229910052697 platinum Inorganic materials 0.000 description 6
- GWEVSGVZZGPLCZ-UHFFFAOYSA-N Titan oxide Chemical compound O=[Ti]=O GWEVSGVZZGPLCZ-UHFFFAOYSA-N 0.000 description 5
- 150000002739 metals Chemical class 0.000 description 5
- TWNQGVIAIRXVLR-UHFFFAOYSA-N oxo(oxoalumanyloxy)alumane Chemical compound O=[Al]O[Al]=O TWNQGVIAIRXVLR-UHFFFAOYSA-N 0.000 description 5
- PXHVJJICTQNCMI-UHFFFAOYSA-N Nickel Chemical compound [Ni] PXHVJJICTQNCMI-UHFFFAOYSA-N 0.000 description 4
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 4
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 4
- 239000003153 chemical reaction reagent Substances 0.000 description 4
- 238000004587 chromatography analysis Methods 0.000 description 4
- 238000004821 distillation Methods 0.000 description 4
- 239000001301 oxygen Substances 0.000 description 4
- 229910052760 oxygen Inorganic materials 0.000 description 4
- 229910052763 palladium Inorganic materials 0.000 description 4
- 229910052703 rhodium Inorganic materials 0.000 description 4
- 239000010948 rhodium Substances 0.000 description 4
- MHOVAHRLVXNVSD-UHFFFAOYSA-N rhodium atom Chemical compound [Rh] MHOVAHRLVXNVSD-UHFFFAOYSA-N 0.000 description 4
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 3
- VYZAMTAEIAYCRO-UHFFFAOYSA-N Chromium Chemical compound [Cr] VYZAMTAEIAYCRO-UHFFFAOYSA-N 0.000 description 3
- 238000007792 addition Methods 0.000 description 3
- 239000006227 byproduct Substances 0.000 description 3
- 229910002092 carbon dioxide Inorganic materials 0.000 description 3
- 239000001569 carbon dioxide Substances 0.000 description 3
- 229910052804 chromium Inorganic materials 0.000 description 3
- 239000011651 chromium Substances 0.000 description 3
- 239000013067 intermediate product Substances 0.000 description 3
- 239000000463 material Substances 0.000 description 3
- 239000001294 propane Substances 0.000 description 3
- 238000000746 purification Methods 0.000 description 3
- 230000035484 reaction time Effects 0.000 description 3
- 238000000926 separation method Methods 0.000 description 3
- 239000007787 solid Substances 0.000 description 3
- 239000000126 substance Substances 0.000 description 3
- 238000006277 sulfonation reaction Methods 0.000 description 3
- 229910052723 transition metal Inorganic materials 0.000 description 3
- 150000003624 transition metals Chemical class 0.000 description 3
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 3
- 239000002028 Biomass Substances 0.000 description 2
- LCGLNKUTAGEVQW-UHFFFAOYSA-N Dimethyl ether Chemical compound COC LCGLNKUTAGEVQW-UHFFFAOYSA-N 0.000 description 2
- OTMSDBZUPAUEDD-UHFFFAOYSA-N Ethane Chemical compound CC OTMSDBZUPAUEDD-UHFFFAOYSA-N 0.000 description 2
- XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical compound [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 description 2
- ZOKXTWBITQBERF-UHFFFAOYSA-N Molybdenum Chemical compound [Mo] ZOKXTWBITQBERF-UHFFFAOYSA-N 0.000 description 2
- UCKMPCXJQFINFW-UHFFFAOYSA-N Sulphide Chemical compound [S-2] UCKMPCXJQFINFW-UHFFFAOYSA-N 0.000 description 2
- 150000001335 aliphatic alkanes Chemical class 0.000 description 2
- PNEYBMLMFCGWSK-UHFFFAOYSA-N aluminium oxide Inorganic materials [O-2].[O-2].[O-2].[Al+3].[Al+3] PNEYBMLMFCGWSK-UHFFFAOYSA-N 0.000 description 2
- 239000001273 butane Substances 0.000 description 2
- 229910052799 carbon Inorganic materials 0.000 description 2
- 239000000571 coke Substances 0.000 description 2
- 238000002485 combustion reaction Methods 0.000 description 2
- 238000001816 cooling Methods 0.000 description 2
- 238000005516 engineering process Methods 0.000 description 2
- 239000012535 impurity Substances 0.000 description 2
- CPLXHLVBOLITMK-UHFFFAOYSA-N magnesium oxide Inorganic materials [Mg]=O CPLXHLVBOLITMK-UHFFFAOYSA-N 0.000 description 2
- 239000000395 magnesium oxide Substances 0.000 description 2
- AXZKOIWUVFPNLO-UHFFFAOYSA-N magnesium;oxygen(2-) Chemical compound [O-2].[Mg+2] AXZKOIWUVFPNLO-UHFFFAOYSA-N 0.000 description 2
- 150000004706 metal oxides Chemical class 0.000 description 2
- 229910052976 metal sulfide Inorganic materials 0.000 description 2
- 229910052750 molybdenum Inorganic materials 0.000 description 2
- 239000011733 molybdenum Substances 0.000 description 2
- IJDNQMDRQITEOD-UHFFFAOYSA-N n-butane Chemical compound CCCC IJDNQMDRQITEOD-UHFFFAOYSA-N 0.000 description 2
- OFBQJSOFQDEBGM-UHFFFAOYSA-N n-pentane Natural products CCCCC OFBQJSOFQDEBGM-UHFFFAOYSA-N 0.000 description 2
- 239000003345 natural gas Substances 0.000 description 2
- 229910052759 nickel Inorganic materials 0.000 description 2
- 239000003209 petroleum derivative Substances 0.000 description 2
- 239000011347 resin Substances 0.000 description 2
- 229920005989 resin Polymers 0.000 description 2
- 239000000377 silicon dioxide Substances 0.000 description 2
- 235000012239 silicon dioxide Nutrition 0.000 description 2
- 230000002194 synthesizing effect Effects 0.000 description 2
- 239000004408 titanium dioxide Substances 0.000 description 2
- 231100000331 toxic Toxicity 0.000 description 2
- 230000002588 toxic effect Effects 0.000 description 2
- 239000010457 zeolite Substances 0.000 description 2
- 229910004385 CaHg Inorganic materials 0.000 description 1
- WGLPBDUCMAPZCE-UHFFFAOYSA-N Trioxochromium Chemical compound O=[Cr](=O)=O WGLPBDUCMAPZCE-UHFFFAOYSA-N 0.000 description 1
- QCWXUUIWCKQGHC-UHFFFAOYSA-N Zirconium Chemical compound [Zr] QCWXUUIWCKQGHC-UHFFFAOYSA-N 0.000 description 1
- 238000009825 accumulation Methods 0.000 description 1
- 239000000654 additive Substances 0.000 description 1
- 230000000996 additive effect Effects 0.000 description 1
- 229910000272 alkali metal oxide Inorganic materials 0.000 description 1
- 150000001340 alkali metals Chemical class 0.000 description 1
- 229910001860 alkaline earth metal hydroxide Inorganic materials 0.000 description 1
- 229910045601 alloy Inorganic materials 0.000 description 1
- 239000000956 alloy Substances 0.000 description 1
- 230000009286 beneficial effect Effects 0.000 description 1
- 150000001721 carbon Chemical group 0.000 description 1
- QGJOPFRUJISHPQ-NJFSPNSNSA-N carbon disulfide-14c Chemical compound S=[14C]=S QGJOPFRUJISHPQ-NJFSPNSNSA-N 0.000 description 1
- 238000009903 catalytic hydrogenation reaction Methods 0.000 description 1
- 239000003610 charcoal Substances 0.000 description 1
- 239000007795 chemical reaction product Substances 0.000 description 1
- 229910000423 chromium oxide Inorganic materials 0.000 description 1
- -1 clays Chemical compound 0.000 description 1
- 239000003245 coal Substances 0.000 description 1
- 229910017052 cobalt Inorganic materials 0.000 description 1
- 239000010941 cobalt Substances 0.000 description 1
- GUTLYIVDDKVIGB-UHFFFAOYSA-N cobalt atom Chemical compound [Co] GUTLYIVDDKVIGB-UHFFFAOYSA-N 0.000 description 1
- 238000007796 conventional method Methods 0.000 description 1
- 238000005336 cracking Methods 0.000 description 1
- 125000004122 cyclic group Chemical group 0.000 description 1
- 238000000354 decomposition reaction Methods 0.000 description 1
- 238000007872 degassing Methods 0.000 description 1
- 230000001419 dependent effect Effects 0.000 description 1
- GDVKFRBCXAPAQJ-UHFFFAOYSA-A dialuminum;hexamagnesium;carbonate;hexadecahydroxide Chemical compound [OH-].[OH-].[OH-].[OH-].[OH-].[OH-].[OH-].[OH-].[OH-].[OH-].[OH-].[OH-].[OH-].[OH-].[OH-].[OH-].[Mg+2].[Mg+2].[Mg+2].[Mg+2].[Mg+2].[Mg+2].[Al+3].[Al+3].[O-]C([O-])=O GDVKFRBCXAPAQJ-UHFFFAOYSA-A 0.000 description 1
- 150000002019 disulfides Chemical class 0.000 description 1
- 229940079593 drug Drugs 0.000 description 1
- 239000003814 drug Substances 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 239000000945 filler Substances 0.000 description 1
- 238000007710 freezing Methods 0.000 description 1
- 230000008014 freezing Effects 0.000 description 1
- 238000003958 fumigation Methods 0.000 description 1
- 238000004817 gas chromatography Methods 0.000 description 1
- 229960001545 hydrotalcite Drugs 0.000 description 1
- 229910001701 hydrotalcite Inorganic materials 0.000 description 1
- 229910052588 hydroxylapatite Inorganic materials 0.000 description 1
- CBOIHMRHGLHBPB-UHFFFAOYSA-N hydroxymethyl Chemical compound O[CH2] CBOIHMRHGLHBPB-UHFFFAOYSA-N 0.000 description 1
- 238000009434 installation Methods 0.000 description 1
- 230000003993 interaction Effects 0.000 description 1
- 229910052742 iron Inorganic materials 0.000 description 1
- 231100000053 low toxicity Toxicity 0.000 description 1
- 238000005259 measurement Methods 0.000 description 1
- 239000012528 membrane Substances 0.000 description 1
- 229910044991 metal oxide Inorganic materials 0.000 description 1
- 239000003921 oil Substances 0.000 description 1
- RVTZCBVAJQQJTK-UHFFFAOYSA-N oxygen(2-);zirconium(4+) Chemical class [O-2].[O-2].[Zr+4] RVTZCBVAJQQJTK-UHFFFAOYSA-N 0.000 description 1
- XYJRXVWERLGGKC-UHFFFAOYSA-D pentacalcium;hydroxide;triphosphate Chemical compound [OH-].[Ca+2].[Ca+2].[Ca+2].[Ca+2].[Ca+2].[O-]P([O-])([O-])=O.[O-]P([O-])([O-])=O.[O-]P([O-])([O-])=O XYJRXVWERLGGKC-UHFFFAOYSA-D 0.000 description 1
- 239000003208 petroleum Substances 0.000 description 1
- 239000000376 reactant Substances 0.000 description 1
- 230000001105 regulatory effect Effects 0.000 description 1
- 229920006395 saturated elastomer Polymers 0.000 description 1
- 239000003079 shale oil Substances 0.000 description 1
- HBMJWWWQQXIZIP-UHFFFAOYSA-N silicon carbide Chemical compound [Si+]#[C-] HBMJWWWQQXIZIP-UHFFFAOYSA-N 0.000 description 1
- 229910010271 silicon carbide Inorganic materials 0.000 description 1
- 239000002689 soil Substances 0.000 description 1
- 238000000629 steam reforming Methods 0.000 description 1
- 238000003860 storage Methods 0.000 description 1
- 150000003464 sulfur compounds Chemical class 0.000 description 1
- 238000001308 synthesis method Methods 0.000 description 1
- 239000011269 tar Substances 0.000 description 1
- OGIDPMRJRNCKJF-UHFFFAOYSA-N titanium oxide Inorganic materials [Ti]=O OGIDPMRJRNCKJF-UHFFFAOYSA-N 0.000 description 1
- 230000009466 transformation Effects 0.000 description 1
- WFKWXMTUELFFGS-UHFFFAOYSA-N tungsten Chemical compound [W] WFKWXMTUELFFGS-UHFFFAOYSA-N 0.000 description 1
- 229910052721 tungsten Inorganic materials 0.000 description 1
- 239000010937 tungsten Substances 0.000 description 1
- 229910052726 zirconium Inorganic materials 0.000 description 1
- 229910001928 zirconium oxide Inorganic materials 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C319/00—Preparation of thiols, sulfides, hydropolysulfides or polysulfides
- C07C319/22—Preparation of thiols, sulfides, hydropolysulfides or polysulfides of hydropolysulfides or polysulfides
- C07C319/24—Preparation of thiols, sulfides, hydropolysulfides or polysulfides of hydropolysulfides or polysulfides by reactions involving the formation of sulfur-to-sulfur bonds
-
- C—CHEMISTRY; METALLURGY
- C01—INORGANIC CHEMISTRY
- C01B—NON-METALLIC ELEMENTS; COMPOUNDS THEREOF; METALLOIDS OR COMPOUNDS THEREOF NOT COVERED BY SUBCLASS C01C
- C01B32/00—Carbon; Compounds thereof
- C01B32/70—Compounds containing carbon and sulfur, e.g. thiophosgene
- C01B32/72—Carbon disulfide
- C01B32/75—Preparation by reacting sulfur or sulfur compounds with hydrocarbons
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C319/00—Preparation of thiols, sulfides, hydropolysulfides or polysulfides
- C07C319/02—Preparation of thiols, sulfides, hydropolysulfides or polysulfides of thiols
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C319/00—Preparation of thiols, sulfides, hydropolysulfides or polysulfides
- C07C319/02—Preparation of thiols, sulfides, hydropolysulfides or polysulfides of thiols
- C07C319/06—Preparation of thiols, sulfides, hydropolysulfides or polysulfides of thiols from sulfides, hydropolysulfides or polysulfides
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C321/00—Thiols, sulfides, hydropolysulfides or polysulfides
- C07C321/02—Thiols having mercapto groups bound to acyclic carbon atoms
- C07C321/04—Thiols having mercapto groups bound to acyclic carbon atoms of an acyclic saturated carbon skeleton
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C321/00—Thiols, sulfides, hydropolysulfides or polysulfides
- C07C321/12—Sulfides, hydropolysulfides, or polysulfides having thio groups bound to acyclic carbon atoms
- C07C321/14—Sulfides, hydropolysulfides, or polysulfides having thio groups bound to acyclic carbon atoms of an acyclic saturated carbon skeleton
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01J—CHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
- B01J2219/00—Chemical, physical or physico-chemical processes in general; Their relevant apparatus
- B01J2219/00002—Chemical plants
- B01J2219/00027—Process aspects
- B01J2219/00029—Batch processes
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01J—CHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
- B01J2219/00—Chemical, physical or physico-chemical processes in general; Their relevant apparatus
- B01J2219/00002—Chemical plants
- B01J2219/00027—Process aspects
- B01J2219/00033—Continuous processes
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y02—TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
- Y02P—CLIMATE CHANGE MITIGATION TECHNOLOGIES IN THE PRODUCTION OR PROCESSING OF GOODS
- Y02P20/00—Technologies relating to chemical industry
- Y02P20/50—Improvements relating to the production of bulk chemicals
- Y02P20/582—Recycling of unreacted starting or intermediate materials
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Inorganic Chemistry (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Low-Molecular Organic Synthesis Reactions Using Catalysts (AREA)
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| FR1456440A FR3023288B1 (fr) | 2014-07-04 | 2014-07-04 | Procede de preparation de disulfure de dimethyle |
| PCT/FR2015/051761 WO2016001554A1 (fr) | 2014-07-04 | 2015-06-29 | Procédé de préparation de disulfure de diméthyle |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| UA119780C2 true UA119780C2 (uk) | 2019-08-12 |
Family
ID=53191729
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| UAA201700970A UA119780C2 (uk) | 2014-07-04 | 2015-06-29 | Спосіб одержання диметилдисульфіду |
Country Status (21)
| Country | Link |
|---|---|
| US (1) | US10550077B2 (ko) |
| EP (1) | EP3164382B1 (ko) |
| JP (2) | JP6698557B2 (ko) |
| KR (2) | KR102174870B1 (ko) |
| CN (1) | CN107074758B (ko) |
| AU (1) | AU2015282544B2 (ko) |
| BR (1) | BR112016030334B1 (ko) |
| CA (1) | CA2952754C (ko) |
| EA (1) | EA031103B1 (ko) |
| ES (1) | ES2714904T3 (ko) |
| FR (1) | FR3023288B1 (ko) |
| MX (1) | MX2016016716A (ko) |
| MY (1) | MY181193A (ko) |
| NZ (1) | NZ727771A (ko) |
| PH (1) | PH12016502484A1 (ko) |
| PL (1) | PL3164382T3 (ko) |
| SG (1) | SG11201610786TA (ko) |
| TR (1) | TR201903045T4 (ko) |
| UA (1) | UA119780C2 (ko) |
| WO (1) | WO2016001554A1 (ko) |
| ZA (1) | ZA201608778B (ko) |
Families Citing this family (5)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| FR3023288B1 (fr) * | 2014-07-04 | 2016-07-15 | Arkema France | Procede de preparation de disulfure de dimethyle |
| WO2022023365A1 (en) | 2020-07-28 | 2022-02-03 | Totalenergies Se | Process to conduct an endothermic thio-reforming reaction of hydrocarbons in an installation comprising electrified fluidized bed reactor |
| FR3122876B1 (fr) | 2021-05-11 | 2024-03-08 | Arkema France | Procédé de co-production d’alkylmercaptan et de dialkyldisulfure à partir d’alcool |
| EP4101815A1 (en) | 2021-06-10 | 2022-12-14 | Evonik Operations GmbH | Hydrogen sulfide reforming of hydrocarbons |
| EP4169895A1 (en) * | 2021-10-21 | 2023-04-26 | TotalEnergies OneTech | Process and catalyst for conversion of carbon disulphide into c2-c3 olefins |
Family Cites Families (33)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2668752A (en) * | 1949-11-09 | 1954-02-09 | Fmc Corp | Process for the production of carbon disulfide |
| US2788262A (en) * | 1953-05-01 | 1957-04-09 | Pan American Petroleum Corp | Process for preparation of carbon disulfide |
| FR1412376A (fr) | 1963-09-23 | 1965-10-01 | Aquitaine Petrole | Nouveau procédé pour la fabrication de mercaptans |
| GB1126465A (en) | 1964-09-14 | 1968-09-05 | Ivor Gray Nixon | Manufacture of hydrogen and carbon disulphide |
| FR2130985A5 (ko) * | 1971-03-29 | 1972-11-10 | Aquitaine Petrole | |
| US3880933A (en) * | 1973-05-02 | 1975-04-29 | Phillips Petroleum Co | Hydrogenation of carbon disulfide to methyl mercaptan in presence of hydrogen sulfide |
| US4481181A (en) * | 1982-02-08 | 1984-11-06 | Ga Technologies Inc. | Hydrogen production from in situ partial burning of H2 S |
| ATE59634T1 (de) * | 1985-05-13 | 1991-01-15 | Atochem North America | Verfahren zur herstellung von dialkyldisulfiden. |
| DE68900007D1 (de) | 1988-04-14 | 1990-10-04 | Elf Aquitaine | Verfahren zur herstellung von organischen di- und polysulfiden. |
| US4822938A (en) | 1988-05-03 | 1989-04-18 | Mobil Oil Corporation | Processes for converting methane to higher molecular weight hydrocarbons via sulfur-containing intermediates |
| FR2659079A1 (fr) * | 1990-03-05 | 1991-09-06 | Elf Aquitaine | Procede pour la fabrication de disulfures organiques. |
| FR2781795B1 (fr) | 1998-07-31 | 2000-09-08 | Atochem Elf Sa | Compositions a base de dimethyldisulfure a odeur masquee |
| DE19854427A1 (de) * | 1998-11-25 | 2000-05-31 | Basf Ag | Verfahren zur Herstellung von organischen Disulfiden |
| CA2412057A1 (en) | 2000-06-14 | 2001-12-20 | University Of Wyoming | Apparatus and method for production of methanethiol |
| FR2844208B1 (fr) | 2002-09-06 | 2004-10-15 | Atofina | Purification du h2s par supports poreux |
| WO2004043883A2 (en) | 2002-11-06 | 2004-05-27 | Georgia-Pacific Resins, Inc. | Conversion of carbon disulfide and hydrogen to methyl mercaptans |
| DE10319739A1 (de) | 2003-04-30 | 2004-11-18 | Basf Ag | Katalysator zur Herstellung von Methylmercaptan aus Methanol und Schwefelwasserstoff |
| RU2394023C2 (ru) | 2003-10-10 | 2010-07-10 | Эвоник Дегусса Гмбх | Способ получения метилмеркаптана |
| US7455828B2 (en) * | 2004-03-01 | 2008-11-25 | H2S Technologies, Ltd. | Process and apparatus for converting hydrogen sulfide into hydrogen and sulfur |
| DE102004037739A1 (de) | 2004-08-04 | 2006-03-16 | Degussa Ag | Wolframat enthaltende Katalysatoren zur Synthese von Alkylmercaptan und Verfahren zu ihrer Herstellung |
| JP4666985B2 (ja) * | 2004-09-28 | 2011-04-06 | 国立大学法人北見工業大学 | 低級炭化水素の直接分解装置 |
| US7897292B2 (en) * | 2005-05-18 | 2011-03-01 | Lilliputian Systems, Inc. | Fuel cell apparatus and methods |
| DE102005043151A1 (de) | 2005-09-10 | 2007-03-22 | Degussa Ag | Verfahren zur Herstellung von Methylmercaptan |
| CN101143329A (zh) | 2006-09-11 | 2008-03-19 | 德古萨股份公司 | Mo-O-K基催化剂、其制备方法及其在甲硫醇合成中的应用 |
| US7645906B2 (en) | 2007-03-27 | 2010-01-12 | Chevron Phillips Chemical Company Lp | Graded catalyst bed for methyl mercaptan synthesis |
| DE102007024576A1 (de) | 2007-05-25 | 2009-05-20 | Evonik Degussa Gmbh | Verfahren zur kontinuierlichen Herstellung von Methylmercaptan aus kohlenstoff- und wasserstoffhaltigen Verbindungen |
| CN101468310B (zh) | 2007-12-28 | 2016-11-16 | 赢创德固赛有限责任公司 | 用于从高H2S合成气合成甲硫醇的负载型Mo-O-K-MexOy催化剂 |
| FR2937566B1 (fr) * | 2008-10-24 | 2014-07-18 | Arkema France | Catalyseur d'hydrogenation, notamment de sulfure de carbone |
| WO2010102653A1 (en) * | 2009-03-13 | 2010-09-16 | Eni S.P.A. | Process for the abatement of hydrogen sulphide from compositions containing it with simultaneous production of hydrogen |
| DE102009027837A1 (de) * | 2009-07-20 | 2011-01-27 | Evonik Degussa Gmbh | Verfahren zur kontinuierlichen Herstellung von Methylmercaptan aus kohlenstoffhaltigen Verbindungen, Schwefel und Wasserstoff |
| EP2751276B1 (en) | 2011-09-02 | 2023-01-25 | Arkema France | Preparation process of l-methionine |
| EP2606967A1 (de) | 2011-12-19 | 2013-06-26 | Evonik Degussa GmbH | Katalysator zur Synthese von Alkylmercaptanen und Verfahren zu seiner Herstellung |
| FR3023288B1 (fr) * | 2014-07-04 | 2016-07-15 | Arkema France | Procede de preparation de disulfure de dimethyle |
-
2014
- 2014-07-04 FR FR1456440A patent/FR3023288B1/fr active Active
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- 2015-06-29 WO PCT/FR2015/051761 patent/WO2016001554A1/fr active Application Filing
- 2015-06-29 US US15/323,564 patent/US10550077B2/en active Active
- 2015-06-29 TR TR2019/03045T patent/TR201903045T4/tr unknown
- 2015-06-29 EA EA201692500A patent/EA031103B1/ru not_active IP Right Cessation
- 2015-06-29 UA UAA201700970A patent/UA119780C2/uk unknown
- 2015-06-29 PL PL15736579T patent/PL3164382T3/pl unknown
- 2015-06-29 NZ NZ727771A patent/NZ727771A/en unknown
- 2015-06-29 CN CN201580036343.6A patent/CN107074758B/zh active Active
- 2015-06-29 KR KR1020197002401A patent/KR102174870B1/ko active IP Right Grant
- 2015-06-29 EP EP15736579.2A patent/EP3164382B1/fr active Active
- 2015-06-29 AU AU2015282544A patent/AU2015282544B2/en active Active
- 2015-06-29 CA CA2952754A patent/CA2952754C/fr active Active
- 2015-06-29 KR KR1020177001995A patent/KR20170021863A/ko not_active Application Discontinuation
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| Publication number | Publication date |
|---|---|
| KR20170021863A (ko) | 2017-02-28 |
| FR3023288B1 (fr) | 2016-07-15 |
| US10550077B2 (en) | 2020-02-04 |
| CA2952754A1 (fr) | 2016-01-07 |
| WO2016001554A1 (fr) | 2016-01-07 |
| EA201692500A1 (ru) | 2017-04-28 |
| JP2017519790A (ja) | 2017-07-20 |
| CN107074758A (zh) | 2017-08-18 |
| MY181193A (en) | 2020-12-21 |
| PL3164382T3 (pl) | 2019-07-31 |
| KR20190011334A (ko) | 2019-02-01 |
| EA031103B1 (ru) | 2018-11-30 |
| NZ727771A (en) | 2020-08-28 |
| AU2015282544A1 (en) | 2017-01-12 |
| ZA201608778B (en) | 2018-05-30 |
| AU2015282544B2 (en) | 2017-09-14 |
| SG11201610786TA (en) | 2017-01-27 |
| MX2016016716A (es) | 2017-04-13 |
| EP3164382A1 (fr) | 2017-05-10 |
| TR201903045T4 (tr) | 2019-03-21 |
| JP6698557B2 (ja) | 2020-05-27 |
| FR3023288A1 (fr) | 2016-01-08 |
| PH12016502484B1 (en) | 2017-04-10 |
| JP2019048840A (ja) | 2019-03-28 |
| CA2952754C (fr) | 2018-11-06 |
| BR112016030334B1 (pt) | 2021-03-23 |
| KR102174870B1 (ko) | 2020-11-05 |
| ES2714904T3 (es) | 2019-05-30 |
| EP3164382B1 (fr) | 2019-01-16 |
| US20170144966A1 (en) | 2017-05-25 |
| PH12016502484A1 (en) | 2017-04-10 |
| CN107074758B (zh) | 2021-02-26 |
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